Interleukin 28B polymorphism impact on early HCV kinetics in HCV-infected liver transplant recipients undergoing antiviral therapy

Aim. To estimate the impact of recipient IL28B genotypes on rapid (RVR) and early virologic responses (EVR) pattern in liver transplant recipients undergoing antiviral treatment (AVT).Material and methods. Blood samples were screened for single nucleotide polymorphisms (SNP) near the IL28B genes (rs...

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Main Authors: V. E. Syutkin, V. P. Chulanov, I. V. Karandashova, V. A. Dolgin, A. O. Chugunov
Format: Article
Language:Russian
Published: Gastro LLC 2011-12-01
Series:Российский журнал гастроэнтерологии, гепатологии, колопроктологии
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Online Access:https://www.gastro-j.ru/jour/article/view/1475
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author V. E. Syutkin
V. P. Chulanov
I. V. Karandashova
V. A. Dolgin
A. O. Chugunov
author_facet V. E. Syutkin
V. P. Chulanov
I. V. Karandashova
V. A. Dolgin
A. O. Chugunov
author_sort V. E. Syutkin
collection DOAJ
description Aim. To estimate the impact of recipient IL28B genotypes on rapid (RVR) and early virologic responses (EVR) pattern in liver transplant recipients undergoing antiviral treatment (AVT).Material and methods. Blood samples were screened for single nucleotide polymorphisms (SNP) near the IL28B genes (rs8099917 T ≥G and rs12979860 C>T) by kit «AmpliSens® Genoscreen-IL28B-FL» (CRIE) in 24 HCV-infected recipients. All the patients underwent pegylated interferon-alfa with (n=21) or without (n=3) ribavirin at least for 12 weeks.Results. Five recipients achieved RVR (one has HCV genotype 1 and 4 patients – HCV genotype 2 or 3) and other 10 – complete EVR. In 6 cases slow virologic response (aviremia between 12 and 24 weeks of treatment, SlVR) occurred. Three patients remained non-responders. G-allele (rs80999917) was present in 3 (20%) out of 15 pts. with complete EVR and in 5 out of 6patients with SlVR (p=0.014). Genotype C/C (rs12979860) was present in 6 (40%) patients with complete EVR and in none of slow-responders (one-sided p=0.041).The groups of recipients with and without complete EVR were comparable with sex, age, pre-treatment viral load, immunosuppression (cyclosporine vs. tacrolimus), weight and body mass index, and mean ribavirin dose. The only pre-treatment factors which have impact on complete EVR were genotype (1 vs. non-1) and IL28B polymorphisms.Conclusion. The SNP in IL28B region may predict slow response to AT in post-LTx setting and should be considered when AT duration is planning.
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spelling doaj-art-236c8992d77241c18eb397e68d25636a2025-02-10T16:14:31ZrusGastro LLCРоссийский журнал гастроэнтерологии, гепатологии, колопроктологии1382-43762658-66732011-12-012164955999Interleukin 28B polymorphism impact on early HCV kinetics in HCV-infected liver transplant recipients undergoing antiviral therapyV. E. SyutkinV. P. ChulanovI. V. KarandashovaV. A. DolginA. O. ChugunovAim. To estimate the impact of recipient IL28B genotypes on rapid (RVR) and early virologic responses (EVR) pattern in liver transplant recipients undergoing antiviral treatment (AVT).Material and methods. Blood samples were screened for single nucleotide polymorphisms (SNP) near the IL28B genes (rs8099917 T ≥G and rs12979860 C>T) by kit «AmpliSens® Genoscreen-IL28B-FL» (CRIE) in 24 HCV-infected recipients. All the patients underwent pegylated interferon-alfa with (n=21) or without (n=3) ribavirin at least for 12 weeks.Results. Five recipients achieved RVR (one has HCV genotype 1 and 4 patients – HCV genotype 2 or 3) and other 10 – complete EVR. In 6 cases slow virologic response (aviremia between 12 and 24 weeks of treatment, SlVR) occurred. Three patients remained non-responders. G-allele (rs80999917) was present in 3 (20%) out of 15 pts. with complete EVR and in 5 out of 6patients with SlVR (p=0.014). Genotype C/C (rs12979860) was present in 6 (40%) patients with complete EVR and in none of slow-responders (one-sided p=0.041).The groups of recipients with and without complete EVR were comparable with sex, age, pre-treatment viral load, immunosuppression (cyclosporine vs. tacrolimus), weight and body mass index, and mean ribavirin dose. The only pre-treatment factors which have impact on complete EVR were genotype (1 vs. non-1) and IL28B polymorphisms.Conclusion. The SNP in IL28B region may predict slow response to AT in post-LTx setting and should be considered when AT duration is planning.https://www.gastro-j.ru/jour/article/view/1475interleukin 28вpegilated interferonhepatitis c virusearly viral kinetics
spellingShingle V. E. Syutkin
V. P. Chulanov
I. V. Karandashova
V. A. Dolgin
A. O. Chugunov
Interleukin 28B polymorphism impact on early HCV kinetics in HCV-infected liver transplant recipients undergoing antiviral therapy
Российский журнал гастроэнтерологии, гепатологии, колопроктологии
interleukin 28в
pegilated interferon
hepatitis c virus
early viral kinetics
title Interleukin 28B polymorphism impact on early HCV kinetics in HCV-infected liver transplant recipients undergoing antiviral therapy
title_full Interleukin 28B polymorphism impact on early HCV kinetics in HCV-infected liver transplant recipients undergoing antiviral therapy
title_fullStr Interleukin 28B polymorphism impact on early HCV kinetics in HCV-infected liver transplant recipients undergoing antiviral therapy
title_full_unstemmed Interleukin 28B polymorphism impact on early HCV kinetics in HCV-infected liver transplant recipients undergoing antiviral therapy
title_short Interleukin 28B polymorphism impact on early HCV kinetics in HCV-infected liver transplant recipients undergoing antiviral therapy
title_sort interleukin 28b polymorphism impact on early hcv kinetics in hcv infected liver transplant recipients undergoing antiviral therapy
topic interleukin 28в
pegilated interferon
hepatitis c virus
early viral kinetics
url https://www.gastro-j.ru/jour/article/view/1475
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AT ivkarandashova interleukin28bpolymorphismimpactonearlyhcvkineticsinhcvinfectedlivertransplantrecipientsundergoingantiviraltherapy
AT vadolgin interleukin28bpolymorphismimpactonearlyhcvkineticsinhcvinfectedlivertransplantrecipientsundergoingantiviraltherapy
AT aochugunov interleukin28bpolymorphismimpactonearlyhcvkineticsinhcvinfectedlivertransplantrecipientsundergoingantiviraltherapy